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Journal of Clinical Microbiology, January 2001, p. 309-314, Vol. 39, No. 1
Medical Technology Program, Department of Microbiology,
Michigan State University, East Lansing, Michigan
48824-10311; Instituto L. S. Lima,
Bauru, São Paulo, Brazil 17001-9702;
Department of Plant and Microbial Biology, University of
California, Berkeley, California 94720-31023;
and Department of Ophthalmology, Emory University School of
Medicine, Atlanta, Georgia 303224
Received 20 June 2000/Returned for modification 15 August
2000/Accepted 4 September 2000
Lacazia loboi is the last of the classical fungal
pathogens to remain a taxonomic enigma, primarily because it has
resisted cultivation and only causes cutaneous and subcutaneous
infections in humans and dolphins in the New World tropics. To place it
in the evolutionary tree of life, as has been done for the other enigmatic human pathogens Pneumocystis carinii and
Rhinosporidium seeberi, we amplified its 18S small-subunit
ribosomal DNA (SSU rDNA) and 600 bp of its chitin synthase-2 gene. Our
phylogenetic analysis indicated that L. loboi is the sister
taxon of the human dimorphic fungal pathogen Paracoccidioides
brasiliensis and that both species belong with the other
dimorphic fungal pathogens in the order Onygenales. The low nucleotide
variation among three P. brasiliensis 18S SSU rDNA
sequences contrasts with the surprising amount of nucleotide
differences between the two sequences of L. loboi used in
this study, suggesting that the nucleic acid epidemiology of this
hydrophilic pathogen will be rewarding.
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.1.309-314.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Phylogenetic Analysis of Lacazia loboi
Places This Previously Uncharacterized Pathogen within the
Dimorphic Onygenales
*
Corresponding author. Mailing address: Medical
Technology Program, Department of Microbiology, Michigan State
University, East Lansing, MI 48824-1031. Phone: (517) 353-7800. Fax
(517) 432-2006. E-mail: mendoza9{at}msu.edu.
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